Podcasts about lung transplant

Host Patti Tripathi talks to Alpha-1 patient advocate Len Geiger ahead of his ATS 2025 International Conference plenary presentation. He was diagnosed at age 35 with a rare lung disease. He almost lost it all, but Len didn't lose his fight. "Everybody can do something more than they're doing right now," he says.

Eight miles. Two friends. One cause.In this inspiring episode, Jacob Venditti opens up about his life with cystic fibrosis, offering candid updates on his health and the challenges he faces as he prepares for a lung transplant. He emphasizes the vital role of community support and shares how his work with the Live Fearlessly Foundation fuels his mission to empower others. Jacob also sheds light on the rare disease income threshold amendment he's championing, which aims to create more equitable opportunities for patients. The conversation builds toward his upcoming Crossing 4 CF event, showcasing his unwavering resilience and commitment to living fearlessly.The heartfelt conversation continues with Rob Brown. Rob talks about their upcoming 80-mile paddle race aimed at raising awareness for cystic fibrosis (CF). Jacob shares how open ocean paddling has become both a personal passion and a powerful way to connect with the CF community. Rob reflects on his enduring friendship with Jacob and their mutual love for surfing. Together, they highlight the healing power of the ocean—physically, mentally, and emotionally—especially for those living with CF. To connect with Jacob and his team: https://livefearlesslyfoundation.com   Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Watch our podcasts on YouTube: https://www.youtube.com/@laurabonnell1136/featuredThanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

In this special bonus episode of The Aging Well Podcast, Dr. Jeff Armstrong honors National Donate Life Month. His guest, Ann Sidesinger, shares her journey with idiopathic pulmonary fibrosis, detailing her diagnosis, the emotional and physical challenges she faced, and her eventual double lung transplant. Ann discusses the importance of resilience, the support she received during her recovery, and how her outlook on life has changed post-transplant. She emphasizes the significance of organ donation and encourages others to consider becoming donors, highlighting the impact it can have on lives like hers. Ann's story is one of hope, strength, and the determination to live life to the fullest after a life-changing medical experience.For more information on Ann's journey and the amazing work of her transplant team at The Ohio State University Wexner Medical Center's Comprehensive Transplant Center, visit:https://wexnermedical.osu.edu/transplant

The timeline of diagnosis, to possible transplant recipient -- to post-transplant can feel like a whirlwind for patients and caregivers. Marion Marin, a lung transplant recipient, joins the show to discuss how that process went for her! She discusses advocating for yourself, waiting for 'the call' -- and the importance of the community around you when physically and emotionally dealing with a diagnosis! It's the 'Pulmonary Fibrosis' podcast! Brought to you the Wescoe Foundation for Pulmonary Fibrosis and the Pennsylvania IPF Support Network! Find this podcast wherever you get your podcasts! Are you interested in helping advance PF research? If so, consider joining a workgroup! Visit wescoe.org or pfpatientengagement.org for more details!See omnystudio.com/listener for privacy information.

On this episode of JHLT: The Podcast, the Digital Media Editors invite lead author Jan Van Slambrouck, MD, to discuss the paper, “The effect of rewarming ischemia on tissue transcriptome and metabolome signatures: A clinical observational study in lung transplantation.”   Dr. Van Slambrouck is a general surgeon who's just finished his PhD training at the KU Leuven lab of respiratory disease and thoracic surgery in Belgium.   The episode explores:  How rewarming ischemia time (RIT) affects donor lungs, especially on the molecular level The pace of rewarming and how prior literature prepared the team to track and evaluate it Clinical strategies to reduce RIT and directly address molecular changes   For the latest studies from JHLT, visit www.jhltonline.org/current, or, if you're an ISHLT member, access your Journal membership at www.ishlt.org/jhlt.   Those involved in the pulmonary vascular disease space should tune in again later this month for a study on the safety and efficacy of riociguat in patients with PAH.   Don't already get the Journal and want to read along? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.

‘I think we get these invitations from God in moments of crisis to let go and to trust'. Naomi Cowan is the CEO of Equip Mental Health Services she is also a lung transplant survivor. Naomi talks with Lizzie Oakes about the ways she encounters God in her everyday life and of how this has changed since navigating her health crisis. https://www.youtube.com/watch?v=9oQpb-QaWzs - to view Naomi's TV interview on Finding the Light TV with Lizzie Oakes. Support Sanctuary Radio: https://donate.rhemamedia.co.nz/?brand=sanctuarySee omnystudio.com/listener for privacy information.

Michael Armstrong is a 25-year-old pre-law student. He loves to read, paint, play card games and video games. He was diagnosed with CF as an infant. We're going to talk about his CF journey and how life took a turn when he was being evaluated for a lung transplant in 2023 and 2024.   Michael was featured in the 2025 Portraits of cystic fibrosis calendar and our first or second  calendar he was featured when he was about five with his  brother.  Michaels dad, Tom was on our Board of Directors for many years…and I was lucky to see him just the other day.Thanks for sharing your story Michael. Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

Speakers: Vince Klassen & Gerry Smiley It's easy to talk about prayer and conceptions of God from a place of health, but what about when you're on the edge of...

If you lose a child to CF, what does that do to parents? To their identity? And their place in the CF community.  These are hard discussions to have, but for a couple years now Peggy Hawkins has want to share her story on this podcast.Peggy talks about the toll waiting for a transplant takes on a family.  One of the issues was that one of them always had to work, in this case it was her husband, so she stayed with Stephen. Peggy and her husband are the parents of three men. She lives in South Carolina  now but was born and raised in Detroit. Peggy worked as a nurse for 43 years (not in CF).Their oldest son Chris is 37 and their youngest is 31 years old. Stephen who died from complications of CF was the middle child. He died at 29 years old. To get in touch with Peggy you can email her here: stephen65roses@aol.com Please like, subscribe, and comment on our podcasts!Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

On this episode of JHLT: The Podcast, the Digital Media Editors invite lead author Jonathan E. Williams, MD, to discuss the paper, “Ex-Vivo Lung Perfusion: National Trends and Post-Transplant Outcomes.” Dr. Williams is a general surgery resident at the University of Michigan in Ann Arbor, with work focusing on contemporary lung preservation strategies, perfusion techniques, and particularly, EVLP. The episode explores: How the study explores the theory that EVLP use may increase transplant volumes Preserving data quality and other study limitations How to work in fields of study that sometimes yield as many questions as answers For the latest studies from JHLT, visit www.jhltonline.org/current, or, if you're an ISHLT member, access your Journal membership at www.ishlt.org/jhlt. Those on heart transplant teams should tune in again later this month for a study on sympathetic reinnervation in cardiac transplant recipients. Don't already get the Journal and want to read along? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.

Send us a textImagine facing life with a heart-lung transplant and then running marathons. That's the incredible journey of our guest, Mark Black, who overcame a congenital heart defect and found a new lease on life through running. From his first steps in rehab to the triumphant completion of marathons, Mark's story is one of grit, resilience, and the relentless pursuit of personal limits. Join us as Mark shares how he reignited his passion for running and offers a masterclass in perseverance that's sure to inspire.Discover the transformative power of run-walk training techniques that have helped many, including Mark, achieve faster marathon times and improved endurance. We explore the 10-in-1 and 3-minute run/30-second walk intervals, strategies that not only enhance performance but also make the marathon experience more enjoyable. Balancing training with family life is no small feat, yet Mark shares practical insights on how he successfully manages his time, all while recounting some memorable marathon experiences across North America.Ever thought about participating in an Ironman relay with a team of heart transplant recipients? Hear about Mark's extraordinary experience with the Tin Men, where camaraderie and shared determination create an unforgettable race. We also touch on building resilience through life's challenges, including Mark's transition from marathons to other fitness pursuits and his inspiring career in public speaking and writing. Tune in for a session filled with heartwarming stories, practical advice, and a celebration of the human spirit's capacity to overcome the odds. Hydrapatch.com code OTNH10 You can reach out to us at:https://coffeycrewcoaching.comemail: Carla@coffeycrewcoaching.com FB @ Over the Next Hill Fitness GroupIG @coffeycrewcoaching.comand Buy Me a Coffeehttps://www.buymeacoffee.com/Carlauhttps://hydra-patch.com/discount/OTNH20https://rnwy.life code: OTNH15https://jambar.com code: CARLA20

Happy new year from JHLT: The Podcast! On this episode, the Digital Media Editors are joined by ISHLT Director of Marketing + Communications Jess Burke, CAE, to share a little bit about themselves and their backgrounds. Hear about how each of the JHLT Digital Media Editors got involved in transplantation and a little about each of their research and personal interests. For the latest studies from JHLT, visit www.jhltonline.org/current, or, if you're an ISHLT member, access your Journal membership at www.ishlt.org/jhlt. Don't already get the Journal? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.

Send us a message!In this episode Dana interviews Emily Bugay, MS, RD, LD about her career path in clinical nutrition, management and dietetic internship directorship. Emily also shares about her work transitioning the UK Dietetic Internship to a provide that pays their interns!Link to the UK Hospital Dietetic Internship: https://ukhealthcare.uky.edu/dietetics-internship-program Deadline to apply: February 1st through DICAS Work at UK HealthCare: https://ukjobs.uky.edu/Emily Bugay, MS, RD, LD is the Director of Clinical Nutrition and the Dietetic Internship program at University of Kentucky HealthCare. She obtained her Bachelor of Science in Dietetics from Michigan State University, completed her Dietetic Internship at UK HealthCare, and her Master's degree in Health Science with an emphasis in health care management from Northern Kentucky University. Prior to her current role, she worked at UK HealthCare as a Clinical Dietitian in both Cardiology and Heart and Lung Transplant positions. She received the Emerging Dietetic Leader award from the Bluegrass Academy of Nutrition and Dietetics in 2023 and has been a guest speaker for dietetic associations, college courses, and symposiums on topics including Transplant Nutrition, cardiac diets for patients with diabetes, and navigating the dietetics profession. She is an active member of the Academy, the Kentucky state affiliate, and the regional affiliate. Emily is passionate about leadership and mentorship, preparing the next generation of dietitians, and fair compensation for nutrition professionals.

Disclosure: DNS DPG does not endorce the Duke University Clinical Nutrition Fellowship program. Our topic for today's episode is micronutrient considerations following lung transplant.  Lung transplant is a surgical treatment option for some patients living with end stage lung disease.  According to the American Lung Association, the intent of this procedure is to replace diseased lungs with healthy lungs in an effort to improve quality of life for people who have medical diagnoses such as COPD, cystic fibrosis and pulmonary fibrosis.  Our guest, Jenny Harrington, MPH, RDN, CNSC, is a dedicated and accomplished dietitian with experience in clinical nutrition and management. She currently serves as a Dietitian II at the University of California, San Diego, where she plays a crucial role in pre-and post-transplant nutrition assessments and collaborates with a multidisciplinary team to optimize patient care and outcomes. This episode was recorded on 11/9/24 and is hosted by Christina M. Rollins, MBA, MS, RDN, LDN, FAND, CNSC.

On this episode of JHLT: The Podcast, the Digital Media Editors invite lead author Chung-Wai Chow, MD, PhD, FRCPC, to discuss the paper, “Pollution exposure in the first 3 months post transplant is associated with lower baseline FEV1 and higher CLAD risk.” Dr. Chow is a transplant pulmonologist and clinician scientist at the University of Toronto, with work focusing on investigating air pollution's impact on chronic lung diseases and developing improved methods to assess lung function. The episode explores: Measurement methods for home and personal air pollution exposures Specific pollutants like black carbon and their effects on patients after lung transplant Practical advice for mitigating these effects For the latest studies from JHLT, visit www.jhltonline.org/current, or, if you're an ISHLT member, access your Journal membership at www.ishlt.org/jhlt. Those on heart transplant teams should tune in again later this month for a Scandinavian study that performs long-term follow ups with patients on the nephrotoxic effects of CNIs. Don't already get the Journal and want to read along? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.

Jess van Slooten is among the hundreds of Kiwis whose life was saved by receiving an organ transplant. At 22, she was diagnosed with a serious lung condition - which required a lung transplant. She says receiving the transplant has allowed her to continue to live a normal life and enjoy her favourite outdoor activities again. "I've been skiing, I've been climbing mountains - lots of adventurous things that I just never would have been able to believe I could have done." LISTEN ABOVESee omnystudio.com/listener for privacy information.

Global Automation Insights: Bell Layoffs, Claude AI Advances, and Robotic Double Lung Transplant In this episode of Hashtag Trending, host Jim Love discusses various trending topics including Bell's pre-holiday layoffs as part of ongoing restructuring, South Korea leading global automation with the highest robot density, and the world's first fully robotic double lung transplant performed in New York. Additional highlights include the integration of voice capabilities into Anthropic's Claude AI models through Hume AI, and the global advancements in industrial automation. 00:00 Introduction and Host Welcome 00:24 Bell's Pre-Holiday Layoffs and Restructuring 01:59 Anthropic's Claude AI and Voice Integration 03:43 World's First Robotic Double Lung Transplant 04:57 South Korea Leads in Global Automation 06:18 Conclusion and Sign-Off

US lawmakers call for a classified briefing on Turkey's Hamas ties, police in Brazil accuse Jair Bolsonaro of a coup plot, Vladamir Putin confirms Russia's use of hypersonic missile in Ukraine, China and Russia oppose a new UN peacekeeping mission in Haiti, a judge suspends sentencing in the Donald Trump hush money case, while Trump chooses Pam Bondi for Attorney General after Gaetz's withdrawal, a GOP senator moves to eliminate the Department of Education, US Securities and Exchange Commission Chair Gary Gensler will step down after Trump's inauguration, Justin Trudeau offers Canadians a tax break and checks, and a New York hospital performs the first fully robotic double-lung transplant. Sources: https://www.verity.news/

Man steals gold rose from 9/11 memorial... City doctors perform the first fully robotic lung transplant... New MLB stadium in Queens finally has a name full This is the All Local 4pm update for November 21, 2024 377 Thu, 21 Nov 2024 20:18:45 +0000 GEpqRy5UuiJskbu7s9ff3fLmd86u6vGL news 1010 WINS ALL LOCAL news Man steals gold rose from 9/11 memorial... City doctors perform the first fully robotic lung transplant... New MLB stadium in Queens finally has a name The podcast is hyper-focused on local news, issues and events in the New York City area. This podcast's purpose is to give New Yorkers New York news about their neighborhoods and shine a light on the issues happening in their backyard. 2024 © 2021 Audacy, Inc. News

Welcome to today's episode of This Thing Called Life, where we explore the evolving landscape of organ, tissue, and eye donation. Join us as we chat with Andi Johnson, featuring Jennie Wright, a double lung transplant recipient, and her daughter, Siri Imanin.  Jennie, diagnosed with sarcoidosis and pulmonary hypertension, waited a year to be listed for a transplant and another two years to receive the lungs. She recounts the challenges, including antibiotic-resistant infections and the emotional toll on her family. Siri shares how her mother's journey influenced her music and activism, emphasizing the importance of organ donation education in the Black community. They discuss the need for proactive health awareness and the impact of supportive networks on their recovery.   Episode Highlights: Andi Johnson introduces the mother-daughter duo Jennie Wright and Siri Imani, and asks Jennie to share her transplant journey Jennie shared that she had sarcoidosis, and as a result, her lungs were severely damaged, which caused pulmonary hypertension. So before the donation, she had a backpack that had oxygen and a fanny pack that had a heart pump. It took a year to get Jennie listed and two years before she got her transplant Jennie recounts the emotional and physical challenges, including contracting antibiotic-resistant infections and the decision to postpone the transplant due to her condition. Andi asks about the support journey for both mother and daughter Siri, Jennie's daughter answers that she was happy once everything was settled because she recalls the long period where her mother's life felt limited and the journey they had to go through in organ donation. Andi asks Siri, who is an artist, creator, activist, & cultivator, how the journey influences her music and the work that she does from a creative standpoint. Siri answers that it influenced everything and that she grabs inspiration from her mother and grandmother in every way. Siri shares that when they first got the diagnosis, she documented and made music about it. Andi asks Siri to share her favorite memory with her grandmother Andi asks what they would like to share with others, particularly in the black community, after just living through this experience. Siri shares her personal journey of overcoming misinformation and distrust, emphasizing the need for education and awareness. Andi questions what they would like to say to their donor family. Jennie expresses her deep gratitude to the donor family for their selflessness and the opportunity to continue living. Jennie and Siri discuss the activities and experiences they can now enjoy, such as walking and attending events. 3 Key Points: Jennie shared that she had sarcoidosis, and as a result, her lungs were severely damaged, which caused pulmonary hypertension. So before the donation, she had a backpack that had oxygen and a fanny pack that had a heart pump. It took a year to get Jennie listed and two years before she got her transplant because there were certain conditions to be met for her to get the transplant. Siri, Jennie's daughter recalls the long period where her mother's life felt limited and the journey they had to go through in organ donation. Siri is also an artist, creator, activist, & cultivator, and she found inspiration in her mother's journey. Siri shares her personal journey of overcoming misinformation and distrust, emphasizing the need for education and awareness. The conversation touches on the historical context of distrust in the medical system within the Black community and the importance of updating that narrative. Tweetable Quotes: “...with that waiting process, the stars have to be perfectly aligned, because you have to be, to be at the top of the list, you got to be the sickest of the sick, right? But you can't be too sick.” - Andi Johnson “My faith helped to sustain me, and I feel like God showed me a moment on the other side of this. And I just kind of held on to that.” - Jennie Wright “I think a lot of our work with people experiencing homelessness just came from the understanding early that life could take you anywhere, no matter what type of person you are, no matter where you come from, you can place where you just need people.” - Siri Imani “I was always planning on making sure, like, people knew who my mama was, people knew who my grandma was, and really remember because they made it clear who they were in their lifetimes.” - Siri Imani Resources: https://getoffthelist.org/ https://lifepassiton.org/ https://lifepassiton.org/board-of-directors-leadership/ https://www.facebook.com/LifeCenterOH https://www.youtube.com/user/LifeCenterOH https://aopo.org/

On this episode of JHLT: The Podcast, the Digital Media Editors discuss a paper from the October issue of JHLT, entitled “Donor to recipient age matching in lung transplantation: A European experience.” Senior author Andrew Fisher, FRCP, PhD joins the podcast to discuss the paper. You'll hear about: European practices in lung transplantation and the donor population Main findings and takeaways How age disparities in donor matching affect outcomes Extended criteria for older donors For the latest studies from JHLT, visit www.jhltonline.org/current, or, if you're an ISHLT member, access your Journal membership at www.ishlt.org/jhlt. If you haven't yet tuned in for the first October episode of the podcast, scroll back in the episode history for the latest ISHLT guideline on the evaluation and care of cardiac transplant candidates. Don't already get the Journal and want to read along? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.

In 2017 Mandy Wilk felt sharp pains in her abdomen and found out she had stage 4 colorectal cancer. The cancer had spread to her liver and would eventually make its way to her lungs. Last summer, she received a first-of-its-kind double lung transplant at Northwestern Medicine in Chicago, and she's now cancer-free. Reset sits down with Mandy to learn about her journey fighting to be heard by doctors and how she's made medical history. For a full archive of Reset interviews, head over to wbez.org/reset.

Welcome to "Catholic Conversations" on Catholic Spirit Radio! In this episode, host Paul Garcia welcomes back Micah Hardy, who shares his incredible journey of battling sarcoidosis and undergoing a successful double lung transplant. Micah, a devoted husband and father of seven daughters, opens up about his recovery, the role of faith in his journey, and the overwhelming support from his family, church, and community. Micah reflects on the challenges he faced, including moments of doubt in his faith, and how his community's support helped him and his family through difficult times. He also discusses the profound impact of a silent retreat and the wisdom he gained through prayer and introspection. Join us for an inspiring conversation about resilience, faith, and the power of community support. Don't miss this heartfelt episode of "Catholic Conversations" on Catholic Spirit Radio.  

Lisa Dent is joined by Dr. Catherine Myers, lung transplant pulmonologist with the Northwestern Medicine Canning Thoracic Institute, to discuss the successful double-lung transplant that was performed at Northwestern Medicine and what this means for people who suffer from lung cancer.

The combination of Sarcoidosis and Covid proved too much for Wade Tomlinson.  His lungs were wracked with damage from sarcoidosis.  So when he got covid it was the punch his body couldn't handle and he needed to take drastic action.  Wade got on several waiting lists for a lung transplant and then waited for the call.  In episode 121 of the FSr Sarc Fighter Podcast, Wade recounts the moment the call came in and the series of events that led to him becoming a recipient.  Let's just say it wasn't clear-cut.  Listen in as Wade tell his story and brings up to date on how he is feeling six months after his surgery. Also in this podcast -- FSR's Stephanie Mizell joins me for a quick explaination of the Foundation's most recent fundraiser!   Show Notes: Sign up for FSR's 100-Mile Challenge: https://givp.nl/register/MGEluUUb  Wade's Go Fund Me: https://www.gofundme.com/f/support-wade-allie-medical-life-expenses?attribution_id=sl:1bcda970-9100-46d6-884b-82c1a3ee4239&utm_campaign=man_sharesheet_dash&utm_medium=customer&utm_source=copy_link   Support Mark Steier's wife, Caeleigh:  https://stopsarcoidosis.rallybound.org/2024-team-rally-for-sarc/Team/View/193889/Team-Sarc-Mark   MORE FROM JOHN: Cycling with Sarcoidosis http://carlinthecyclist.com/category/cycling-with-sarcoidosis/ Do you like the official song for the Sarc Fighter podcast?  It's also an FSR fundraiser! If you would like to donate in honor of Mark Steier and the song, Zombie, Here is a link to his KISS account.  (Kick In to Stop Sarcoidosis)  100-percent of the money goes to the Foundation.  https://stopsarcoidosis.rallybound.org/MarkSteier The Foundation for Sarcoidosis Research https://www.stopsarcoidosis.org/ Donate to my KISS (Kick In to Stop Sarcoidosis) fund for FSR  https://stopsarcoidosis.rallybound.org/JohnCarlinVsSarcoidosis?fbclid=IwAR1g2ap1i1NCp6bQOYEFwOELdNEeclFmmLLcQQOQX_Awub1oe9bcEjK9P1E My story on Television https://www.stopsarcoidosis.org/news-anchor-sarcoidosis/ email me  carlinagency@gmail.com                              

It has been many moons since we have dropped in with an episode. In this episode we discuss what has transpired with Zest's latest medical rebirth through receiving his second double lung transplant in May. We also address the Indubious "hiatus" in order to answer the burning questions of our beloved Indubious fans. You can check out Zest's solo project "Heaven Zest" at https://www.facebook.com/heavenzest111 and https://open.spotify.com/artist/7uHT0NJJedyIPNx2QOZrwAYou can check out Skip's Iboga retreat center here:www.ibogarebirth.comwww.indubiousmusic.comFacebook: www.facebook.com/indubiousmusicSpotify: https://open.spotify.com/artist/77su9uR4crZ4HOOnCibJwFInstagram: www.instagram.com/indubious

Episode 5 is a an incredible conversation with Bern's daughter Danica. As Bern and I were building our recordings, we realized, the story would not be complete without hearing from her daughter. In this episode, Danica and I explore growing up with a mom with Cystic Fibrosis and the moment the call came for the lung transplant. No doubt, listeners will be blown away by Danica's poise and vulnerability.

On this episode of JHLT: The Podcast, the JHLT Digital Media Editors explore two studies from the July issue of The Journal of Heart and Lung Transplantation. Digital Media Editor Marty Tam, MD, a transplant cardiologist from the University of Michigan in Ann Arbor, hosts this episode.   First, Dr. Tam and Digital Media Editor Erika Lease, MD, FCCP, interview their first guest, Daniel Calabrese, MD, first author on the study “Macrophage and CD8 T cell discordance are associated with acute lung allograft dysfunction progression.” The study's authors sought to tackle challenges behind early detection of chronic lung allograft dysfunction (CLAD) by identifying biomarkers associated with acute lung allograft dysfunction (ALAD) progression to CLAD.   To do this, they collected bronchoalveolar lavage (BAL) cells at the time of ALAD diagnosis and performed single cell RNA sequencing to identify significant differences in 26 unique cell populations across groups, with discordant CD8 T cells and macrophages providing the best discrimination between ALAD with decline from ALAD with recovery and controls.   Dr. Calabrese discusses how his team identified the diagnostic criteria, why the biomarkers might lead ALAD to progress to CLAD, and how the findings might lead to early targeted therapies.   Next, Dr. Tam joins and Digital Media Editor Khue Ton, MD and David Schibilsky, MD, to interview their next guest, David D'Alessandro, MD, the Surgical Director of Cardiac Transplantation and MCS at Massachusetts General Hospital in Boston. Dr. D'Alessandro was the first author on the study “Impact of controlled hypothermic preservation on outcomes following heart transplantation,” which sought to assess the impact of the Paragonix SherpaPak Cardiac Transport System, a device allowing controlled hypothermic  preservation, on rates of primary graft dysfunction (PGD) and post-transplant mortality.   The key finding was that controlled hypothermic preservation was associated with a lower incidence of severe PGD – 6.6% compared to ice storage at 10.4%. In the conversation, Dr. D'Alessandro answers questions about the need for innovation over traditional ice cold storage, the greatest advantages of controlled hypothermic approaches, and the next steps in this research.   Follow along at www.jhltonline.org/current, or, if you're an ISHLT member, access your Journal membership at www.ishlt.org/jhlt.   Don't already get the Journal and want to read along? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.

Today's guest is Jim Stempel. Jim has been a scleroderma warrior for almost 2 decades. For him scleroderma attacked his lungs, resulting in a lung transplant in 2018. He then decided to retire which led him to volunteer. Jim is doing wonderful advocacy for the scleroderma community. Listen to hear his journey and how is giving back.

DAVID WEILL, M.D., is the former Director of the Center for Advanced Lung Disease and Lung and Heart-Lung Transplant Program at Stanford University Medical Center. He is currently the Principal of the Weill Consulting Group which focuses assisting hospitals in improving their transplant programs and developing new programs in the US and throughout the world. David's writing has appeared in the Wall Street Journal, USA Today, Newsweek, and The San Francisco Chronicle. In his new novel, “All That Really Matters,” David explores the demands, challenges and complications of a fictional transplant surgeon. We discuss his 25 year career as a lung transplant surgeon and the behind-the-scenes world of medical ethics, corporate greed in medicine and the life and death decisions made in “the selection room,” where it is decided who gets a transplant and who doesn't. www.davidweill.com

David Weill is the former Director of the Center for Advanced Lung Disease and Lung and Heart-Lung Transplant Program at Stanford University Medical Center. He is currently the Principal of the Weill Consulting Group which focuses on improving the delivery of pulmonary, ICU, and transplant care. David's writing has appeared in the Wall Street Journal, USA Today, Newsweek, the Chicago Tribune, the Washington Post, The Hill, and the Los Angeles Times. He also has appeared on Fox, CNN, the New York Times, the San Francisco Chronicle, and the Wall Street Journal. David's memoir Exhale: Hope, Healing, and A Life in Transplant was published in May of 2021. All That Really Matters is his debut novel. David divides his time between New Orleans and Alys Beach, FL, with his wife, Jackie, two daughters, Hannah and Ava, and their dogs, Lucy and Frannie.

Shortly after we did this podcast Matt died from complications of cystic fibrosis.  With permission from his sisters, and dear friend Jennifer Bleecher (featured in this podcast) we are now airing this podcast to shine a light about what a great man Matt was. He speaks in this podcast about concern for his health.  Thanks to Jenn, his family and to Matt for all he gave to the world and especially the CF community. You are missed and will never be forgotten.From his sisters Molly McBryan and Ame Austin:"After an extremely long hard fought battle with cystic fibrosis, Matt McCloskey succumbed to this terrible disease on February 7th, 2024. He was a beloved husband, son, brother, uncle, and friend to many.   He will be remembered for a lot of things; one of which was his passion for the Take A Breather foundation in which he started.The concept of Take A Breather started for Matt in 2012, when his own health battle with CF really took a turn. Knowing first hand what it is like to live with this disease, it was his dream and vision to offer families living with cystic fibrosis, a temporary escape, a breather, from the everyday struggles and emotional burdens of their disease. Matt put his heart and soul into this Foundation and is truly what drove him despite his own health issues.  Because of Matt, thousands of lives have been forever impacted due to his selflessness of wanting to bring joy to so many living with CF. He worked tirelessly and countless hours for the Take A Breather Foundation and the CF community.  Throughout the years, we heard from  many recipients/families the huge impact Matt's mission had on their lives but we know there were countless others whom we did not hear from because he also worked quietly behind the scenes to motivate, answer questions, or just listen. There are no words to express the profound impact this loss will have on all those who knew and loved him and to the CF community."This was written prior to his passing:Matt and Jen have a great story to tell. Two people with CF, living their separate lives, and then they began working together to make a difference in the lives of people with CF.Matt McCloskey was born in 1968 and grew up in Philadelphia, he has several other siblings, and one he never met because he died from CF at 2 months old.In 2015 Matt received a lung transplant. Matt's in his 50's now, but his life expectancy was 6 years old.He is currently running the Take A Breather Foundation.Jen Bleecher, who is 52 years old, is the Community Outreach Volunteer for Take a Breather.  Jen is married, and has a 27-year-old daughter . Jen worked as a nurse for over 20 years. Jen had a double lung transplant, she has pivoted to volunteering some of her time helping with the Community Outreach initiatives, such as building relationships within the CF and broader communities, assisting in planning of fundraising events, and overseeing Take A Breather's School Club program. To contact Matt and Jen: https://takeabreatherfromcf.orgPlease consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website: https://thebonnellfoundation.orgBonnell Foundation email: thebonnellfoundation@gmail.comThanks to our sponsors:Vertex:  https://www.vrtx.comViatris: https://www.viatris.com/en Please like, subscribe, and comment on our shows, wherever you get your podcasts.Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

  In this special episode of Kent's Kidney Stories, host Kent Bresler steps outside the usual realm of kidney disease to bring you an inspiring conversation with Steven Gambrel, a heart and double lung transplant recipient. Steven shares his remarkable journey, starting from his congenital heart defect diagnosed at birth, through the trials of atrial fibrillation in his teenage years, to the life-saving transplant he received over 29 years ago. Steven candidly discusses the challenges he faced growing up with his condition, the transformative moment of receiving his transplant, and the ongoing battle with immunosuppressive medication. Kent and Steven delve into the unique aspects of living with a heart and double lung transplant, including the physical and mental hurdles, the importance of family support, and the profound impact of organ donation. This episode is a testament to resilience and the power of medical advancements. Steven's story is not only a source of inspiration but also a call to action for greater awareness and support for organ donation. Whether you're a patient, a medical professional, or someone interested in the incredible stories of transplant recipients, this episode offers a deep and heartfelt look into the life of someone who has beaten the odds. For more information on Kidney Solutions and to join their supportive community, visit kidneysolutions.org. Host: Kent Bresler Producer: Jason Nunez Remember to keep breathing, and don't miss the next amazing episodes of Kent's Kidney Stories!

Lung Transplant   Guest: Philip J. Spencer, M.D. Hosts: Malcom Bell, M.D. Lung transplant has evolved over the last 4 decades to be come the only “durable” treatment for end stage lung failure and pulmonary hypertension. Long-term survival remains a challenge however is improving with time while the severity of illness we can treat continues to expand   Topics Discussed: What patients are we currently treating with lung transplantation and how has this changed over time. What tools have evolved over the last 10-15 years that have increased our ability to expand lung transplantation to older and more severely ill patients? What areas do you see as a focus for improvement in the next decade in the field of lung transplantation?   Connect with Mayo Clinic's Cardiovascular Continuing Medical Education online at https://cveducation.mayo.edu or on Twitter @MayoClinicCV and @MayoCVservices. LinkedIn: Mayo Clinic Cardiovascular Services Cardiovascular Education App: The Mayo Clinic Cardiovascular CME App is an innovative educational platform that features cardiology-focused continuing medical education wherever and whenever you need it. Use this app to access other free content and browse upcoming courses. Download it for free in Apple or Google stores today! No CME credit offered for this episode. Podcast episode transcript found here.

Alastair is an author, Narrator, Adventurist, and Double Lung Transplant recipient. Alastair immigrated to Canada from England by himself when he was 19. He became a typical yuppie – family, a house in the suburbs, and a big job in the corporate sector. Following London Life's Freedom 55 plan – he retired at 57 and went to live in the country. Disillusioned with retirement's passivity, he shed his material possessions and lived for two years with a small First Nations band in a remote fly-in location in the Northwest Territories. Cultural differences and a challenging environment ignited in him fresh perspectives, and inspired a new way of being, and fueled his soul searching. The experience changed the direction of his life, which he wrote about in his memoir Awakening in the Northwest Territories. He left the north two years later and, motivated to help others, went to Bangladesh on a two-year assignment as an International Development volunteer. With his new partner, Candas Whitlock, they next went to Jamaica and Guyana as International Development volunteers on one-year assignments. They co-wrote Go For It: Volunteering Adventures on Roads Less Traveled. Two years later, between volunteering assignments, they spent four months backpacking Central America and Southeast Asia and co-wrote Budget Backpacking for Boomers. They were part of a Reconciliation Canada project. In 2016, they went to Alert Bay, B.C., on a four-month volunteer placement with the Namgis First Nations. This was part of a Reconciliation Canada project. The experience was so profound that they felt compelled to write about it in a memoir entitled Tides of Change. Candas and Alastair became entertainers for the next three years, presenting their audio/visual shows based on their books to audiences in retirement residences, service clubs, libraries, and community centers throughout Ontario. Alastair's double lung transplant in 2020 enabled him to finish writing his novel The Soldier and the Orphan and narrate it as an audiobook. While narrating his other books (his three memoirs), he learned that there is a demand for his type of voice–senior male with a British accent – as a narrator and voice-over artist. Alastair has three children and seven grandchildren and lives in London, Ontario. Canada. Learn more about your host, Kim Lengling www.kimlenglingauthor.com --- Send in a voice message: https://podcasters.spotify.com/pod/show/letfearbouncepodcast/message

Do you know what is needed before you have a lung transplant?  Or even how it works?  More and more adult CF clinics are explaining the details to adult patients, but if you're a CF parent, there is a lot you may not know. We welcome Dr. Ryan Hadley. Dr. Hadley is at Corewell health in Grand Rapids. He is an assistant Profession of Medicine in pulmonary and Critical care. He is a published author and researcher some of his academic appointments include Core Faculty with Pulmonary Critical Care Fellowship and MSU, assistant professor in the pulmonary and critical care.His resume is beautifully long.  Here are some of his publications: “Acellular Normal and Fibrotic Human Lung Matrices as a Culture System for In Vitro Investigation” American Journal of Respiratory and Critical Care Medicine, Nov 1 2012, 186(9) 866-876.Adam J. Booth, Ryan Hadley, Ashley M. Cornett, Alyssa A. Dreffs, Stephanie A.Matthes, Jessica L. Tsui, Kevin Weiss, Jeffery C. Horowitz, Vincent F. Fiore, Thomas H. Barker, Bethany B. Moore, Fernando J. Martinez, Laura E. Niklason, and Eric S. White“Idiopathic Non-specific Interstitial Pneumonia” Respirology.  2016 Feb;21(2):259-68.Elizabeth Belloli, Rosemary Beckford, Ryan Hadley, Kevin Flaherty“Critically Ill Patients with Interstitial Lung Disease” Clinics in Chest Medicine.  2015Sep;36(3):497-510.Ryan Hadley, Robert Hyzy Please like, subscribe, and comment on our shows, wherever you get your podcasts.Please consider making a donation: https://thebonnellfoundation.org/donate/The Bonnell Foundation website:https://thebonnellfoundation.orgEmail us at: thebonnellfoundation@gmail.com Thanks to our sponsors:Vertex: https://www.vrtx.comViatris: https://www.viatris.com/en

Carly-Jay Metcalfe lives with cystic fibrosis, and has faced a double lung transplant, a rare cancer and other huge medical challenges. But through it all humour and hope have fuelled her survival (CW: this story discusses organ transplant and donation, drug use and self harm)

Host: Darryl S. Chutka, M.D. [@chutkaMD] Guest: Kelly Pennington, M.D. Guest: Sahar Saddoughi, M.D., Ph.D. The lung is one of the most common organs transplanted, trailing transplants of kidney, liver, and heart, with over 2600 performed in 2022. Lung transplantation may involve transplanting either one or both lungs, and occasionally performed together with a heart transplant. Although some patients with a lung transplant have lived more than 10 years, only about half are alive after 5 years. In this podcast, we'll discuss “When to Refer a Patient for a Lung Transplant”. Who's a candidate for a lung transplant and when should we think about this for our patients? How successful is a lung transplant and what are conditions that would exclude a patient from the procedure? These are all questions I'll be asking my guests, thoracic surgeon, Sahar Saddoughi, M.D., Ph.D., and pulmonologist, Kelly Pennington, M.D., both from the Mayo Clinic in honor of ‘National Donate Life Month'.                  Connect with the Mayo Clinic's School of Continuous Professional Development online at https://ce.mayo.edu/ or on Twitter @MayoMedEd.  https://www.mayoclinic.org/departments-centers/lung-transplant/home/orc-20211835

On this episode of JHLT: The Podcast, the JHLT Digital Media Editors explore two studies from the April issue of The Journal of Heart and Lung Transplantation. Digital Media Editor Erika Lease, MD, a transplant pulmonologist at the University of Washington in Seattle, hosts this episode.   First, Dr. Lease and Digital Media Editor Van-Khue Ton, MD interview their first guests, Paul J. Scheel III, MD and Steven Hsu, MD, both of Johns Hopkins University. Dr. Scheel was first author and Dr. Hsu was senior author on the study “Occult right ventricular dysfunction and right ventricular-vascular uncoupling in left ventricular assist device recipients.” The main finding of the study is that LVAD recipients have depressed intrinsic RV contractility and reduced RV compensation.   Drs. Scheel and Hsu give an overview of RV pressure-volume loops and their measurements, and discuss the impact of LVAD on intrinsic RV contractility, contractile reserve, and vascular coupling. If you want to know how these findings are important to clinical care, you'll need to listen to the episode!   Next, Dr. Lease and Digital Media Editor David Schibilsky, MD, interview their next guest, Joshua Diamond, MD, of the University of Pennsylvania. Dr. Diamond was first author on the study “Development and validation of primary graft dysfunction predictive algorithm for lung transplant candidates.” The authors of the study set out to develop a clinically useful and generalizable PGD prediction model to aid in clinical decision making.   Dr. Diamond discusses the factors they considered in building the model, the model's strengths over other approaches, and its limitations. Tune in to learn more!   Follow along at www.jhltonline.org/current, or, if you're an ISHLT member, access your Journal membership at www.ishlt.org/jhlt.   Don't already get the Journal and want to read along? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.    

DISCLAMER >>>>>>    The Ditch Lab Coat podcast serves solely for general informational purposes and does not serve as a substitute for professional medical services such as medicine or nursing. It does not establish a doctor/patient relationship, and the use of information from the podcast or linked materials is at the user's own risk. The content does not aim to replace professional medical advice, diagnosis, or treatment, and users should promptly seek guidance from healthcare professionals for any medical conditions.                                                  >>>>>> The expressed opinions belong solely to the hosts and guests, and they do not necessarily reflect the views or opinions of the Hospitals, Clinics, Universities, or any other organization associated with the host or guests.                                                                                  Disclosures: Ditch The Lab Coat podcast is produced by (Podkind.co) and is independent of Dr. Bonta's teaching and research roles at McMaster University, Temerty Faculty of Medicine and Queens University. On today's episode of "Ditch the Labcoat," our host Dr. Mark Bonta dives deep with renowned intensive care expert Dr. Niall Ferguson into the world of intensive care, ventilators, and the balance between technology and humanity in critical care medicine.In a compelling conversation, we unlock insights into the evolution of respiratory care, the ethical considerations surrounding life support, and how the COVID-19 pandemic reshaped our approach to patient care.Key takeaways from this episode:- The Overuse of ICU Resources: Dr. Ferguson discusses the careful balance required when utilizing ICU facilities, emphasizing the need for proportionate care to maximize patient dignity and humanity, even in unconscious states.- The Evolution of Ventilation Techniques: Delve into the history of ventilatory support, from the iron lung to modern positive pressure ventilation, and understand how these critical interventions have been both a lifeline and a learning curve during pandemics.- Patient-Centered Care: Drs. Bonta and Ferguson underscore the necessity of clear, honest communication between healthcare providers and patients, aligning treatment with patient health goals, especially when considering life-support interventions.Don't miss the heartfelt stories, professional insights, and the fusion of human touch with technology that Dr. Ferguson brings to this enlightening discussion on "Ditch the Labcoat".Dr. Niall Ferguson shares a compelling tale from medical history, asserting the dramatic impact of vaccines in eradicating polio. He recounts the 1952 polio conference in Copenhagen, which, ironically, preceded a polio outbreak later that year in the same city. This outbreak led to deaths from not just respiratory muscle weakness but from bulbar polio, affecting the victim's ability to swallow and clear secretions. The conventional iron lung was unable to aid patients in coughing or clearing these secretions, resulting in numerous fatalities.However, a pivotal moment in medical innovation emerged when an astute anesthetist named Bjorn Ibsen intervened. Recognizing patients were hypoventilating, Ibsen proposed a more effective method: invasive positive pressure ventilation, an invention that has since revolutionized medical care. This story, relayed by Dr. Ferguson, underscores the relentless pursuit of medical advances in the face of disease outbreaks and the critical role that vaccines play in preventing such health crises.00:00 Ventilator's origin, critical care medicine, teamwork in healthcare.05:24 Vaccines ended polio, led to ventilation innovation.14:45 COVID patients may have low oxygen levels.20:50 Setting up province wide COVID response; challenges.25:20 Mechanical ventilation can cause respiratory damage.28:15 Balancing life support on ventilator, ECMO concerns.37:43 Patients' readiness and family's understanding affect decisions.40:40 Importance of end-of-life conversations for clarity.48:27 Some private hospitals have overly luxurious ICUs.52:18 Doctor prioritizes in-person patient interaction during rounds.54:47 Impactful conversation about ventilator history and medicine.01:00:30 Gratitude and encouragement for future engagement.© 2024 ditchthelabcoat.com - All Rights Reserved 

On this episode of JHLT: The Podcast, the JHLT Digital Media Editors explore two studies from the March issue of The Journal of Heart and Lung Transplantation. Digital Media Editor Marty Tam, MD, an advanced heart failure and transplant cardiologist at University of Michigan in Ann Arbor, hosts this episode.   First, Dr. Tam and Digital Media Editor David Schibilsky, MD interview their first guests, Fiorella Calabrese, MD and Francesca Lunardi, MD, ScD, PhD, of University of Padova, in Padova Italy. Dr. Lunardi was first author and Dr. Calabrese was senior author on the study “Assessing the role of phosphorylated S6 ribosomal protein in the pathological diagnosis of pulmonary antibody-mediated rejection.” In the conversation, Drs. Calabrese and Lunardi share the main challenges in the current diagnostic algorithm for AMR in lung transplantation, and why this protein expression may be a future mainstay in evaluating patients with this condition.   Next, Dr. Tam and Digital Media Editor Van-Khue Ton, MD, interview their next guest, Benjamin Mackie, MD, of Tampa General Hospital. Dr. Mackie was senior author on the study “Relationship between blood and tissue-based rejection-related transcripts in heart transplantation.” In the conversation, Dr. Mackie shares the current state of rejection assessment, including new, non-invasive modalities, and how the relation between these diagnostic methods may inform clinical practice.   Follow along at www.jhltonline.org/current, or, if you're an ISHLT member, access your Journal membership at www.ishlt.org/jhlt.   Don't already get the Journal and want to read along? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.

Join us on a remarkable journey with Alastair Henry, the adventurous boomer and double lung transplant survivor who turned his life around post-retirement. From the corporate boardrooms to the remote Canadian North, to volunteering across the globe, Alastair's story is a testament to living life to the fullest. Discover how he embraced indigenous wisdom, tackled idiopathic pulmonary fibrosis, and found joy in simplicity on this inspiring episode of the Living the Dream podcast with Curveball.

At age 52, Tammy Ecker, was diagnosed with COPD and she has been fully oxygen dependent for years, She was facing End Stage COPD, which has no cure. She was praying for a miracle and got one. She got her miracle two lungs and can joins the podcast with Gene McGuire (honey-doer) to share her success and gratitude. She is 57 and is appreciating life more than ever.  Here is the link for Tamm's go fund me - https://gf.me/u/4br97u And to follow their journey with pictures and videos on: instagram.com/gmacwire/ facebook.com/gene.mcguire.14

In our final episode of 2023, the JHLT Digital Media Editors have two manuscripts from the December 2023 issue of The Journal of Heart and Lung Transplantation! Digital Media Editor Erika Lease, MD, transplant pulmonologist at the University of Washington in Seattle, hosts this episode.   First, a free-ranging conversation with first author Mark E. Snyder, MD, and senior author John F. McDyer, MD, on their team's study “Impact of age and telomere length on circulating T cells and rejection risk after lung transplantation for idiopathic pulmonary fibrosis.”   A subset of patients with idiopathic pulmonary fibrosis (IPF) have a heritable, age-adjusted short telomere length. Mutations in telomere length can manifest as T-cell dysfunction and immunodeficiency. As T-cells are involved in the development of acute cellular rejection (ACR), the authors hypothesized that the combination of age and telomere length would impact the degree of ACR burden in lung transplant recipients—and indeed, the authors found that lung transplant recipients with IPF and short telomere length had premature “aging” of their circulating T-Cells. There was a significant decline in early ACR burden with increasing age, found only in those with short telomere length.   How might these findings impact immunosuppression regimens in clinical practice? What follow-up studies to they have planned? In the discussion, Drs. Snyder and McDyer, both of UPMC in Pittsburgh, discuss all these possibilities, as well as the the work of their collaborator, Jonathan K. Alder, PhD, as inspiration for the study.   Next, the editors explored “Early optical coherence tomography evaluation of donor-transmitted atherosclerosis and cardiac allograft vasculopathy: insights from a prospective, single-center study,” in a discussion with senior author Snehal R. Patel, MD, of the Montefiore Medical Center in New York.   Cardiac allograft vasculopathy (CAV) remains a major cause of death in heart transplant recipients, and donor-transmitted atherosclerosis (defined as a maximal intimal thickness of >/= 0.5mm on baseline intravascular ultrasound (IVUS) early after transplant) is believed to carry a greater risk for the development of CAV. Dr. Patel's team, however, hypothesized that optical coherence tomography (OCT) may have advantages over IVUS as an imaging modality due to its higher resolution. In this prospective, observational study, the authors assessed the prognostic role of OCT, and found that transplant recipients whose OCT imaging showed advanced plaque characteristics had a significantly higher event rate after a mean follow up of 3.3 years. OCT was also an independent predictor of clinic events, while maximal intimal thickness of >/= 0.5mm was not.   In the episode, Dr. Patel shares the key features of OCT that may make it of clinical use, the three risk categories developed for the study, and what the follow-ups might be.   Follow along at www.jhltonline.org/current, or, if you're an ISHLT member, log in at ishlt.org/journal-of-heart-lung-transplantation.  Don't already get the Journal and want to read along? Join the International Society of Heart and Lung Transplantation at www.ishlt.org for a free subscription, or subscribe today at www.jhltonline.org.    

We're back with our Top Consults series to talk about Lung Transplant! This is a topic that every pulmonologist should have background knowledge about since it impacts the care of patients with end-stage lung disease of any cause. We will … Continue reading →

In this riveting podcast episode, we continue the incredible saga of Selwa and her husband, Scott, as they share the pivotal moments in their journey through Selwa's life-threatening battle with Cystic Fibrosis. Chapter 2 explores the paramount importance of advocacy, highlighting the need for a voice when one cannot speak for themselves in the hospital.Selwa reflects on her harrowing experience during her second lung transplant, where her body teetered on the brink of shutdown. Scott, a staunch advocate for his beautiful wife Selwa, envisions a book that can help others navigate the complexities of the healthcare system.Listeners will be drawn into the narrative as Scott describes the heart-wrenching moment when Selwa's health took a drastic turn, leading to a frantic 911 call and a race against time. The podcast delves into the power of prayer, will, and the unwavering support of loved ones that kept Selwa alive during her darkest hours.Discover the pivotal role advocacy played in Selwa's recovery, as Scott bridged the gap between doctors and their patient, providing essential context and history. Selwa's miraculous recovery from multiple organ failures and her journey back from the brink of death will leave you in awe.The episode also sheds light on Selwa's current battle as she strives for a third lung transplant. Join us in exploring her unwavering determination, the compassionate medical teams supporting her, and the incredible strength of her family. Selwa's story is one of resilience, love, and the unyielding pursuit of life against all odds.Hashtags:#SelwasJourney #AdvocacyMatters #MiraculousRecovery #FightForLife #FamilySupport #CysticFibrosisWarrior #ThirdLungTransplant #TriumphOverAdversity #MedicalMiracles #HopeAndResilience #NeverGiveUp

Amy got new lungs and then met Andy Grammar!See omnystudio.com/listener for privacy information.

Today I sit down with Lindsey Roy. I was introduced to her through a mutual connection who thought she would be a great fit to be on the podcast. After some research, I was blown away by her story and was so grateful when she agreed to come on the show.  10 years ago, Lindsey was in a serious boating accident, which lead to an amputation. Then just 10 months ago, she underwent a double lung transplant. Not only has she kept a positive outlook during these trials, but she has continued to win at work, and at home. She is a successful business leader with Hallmark, a wife for 15 years, and a mother to 2 kids. Her story is one of resilience and faith that I think all of us could learn and be encouraged by.   In this episode, you'll discover…  What is the key trait to winning at work and at home? (2:08) Lindsey opens up about her accident. (5:23) How did God show himself during her trauma? 9:17) Lindsey's double lung transplant (15:42) Communication. Express your needs. (26:52) You can't feel grateful and fearful at the same time. (35:24)   Lindsey's Bio: A tragic boating accident while on vacation almost claimed Lindsey¹s life and left her with an amputated left leg, severely injured right leg, and injured right arm. Through a challenging recovery process, Lindsey learned impactful lessons on how to harness disruption and find clarity in the chaos. A fresh voice on the speaking circuit, Lindsey has been heralded for her authentic style and universal message. Lindsey has spent over eighteen years in the corporate environment, leading teams in innovation, digital development, and product merchandising. She was named Vice-President at Hallmark Cards at just thirty-two years old, one of the youngest VPs ever in a company with over a 100-year history, and in the top 1% of brands worldwide. Lindsey combines her unique life experience, corporate background, and emotional intelligence to truly connect with audiences.   What's Next?  Have you read Rise and Go?! Rise and Go is a resource for you to get back up quicker. It was just released on Amazon and Audible. You can find out more about it here! I pray the content helps you as much as it has me and my clients. Thanks for your support in helping leaders win at work and at home! Are you crushing it at work but struggling at home? If you want to learn how to win at home, then go to https://CoryMCarlson.com/subscribe and download your free copy of “10 Ways To Win At Home.” If you're looking for a resource to help you with these times when your work is now in your home, check out my book Win At Home First on Amazon. Forbes Magazine rated it one of 7 books everyone on your team should read.

A mother fights against time and navigates the emotional rollercoaster of her daughter's lung transplant, as she strives to fulfill her promise while facing the heart-wrenching challenges of the organ transplant process in a race for survival. In this episode, you will be able to: Uncover the intricate realities of pediatric lung transplants and management of exceptional medical conditions. Relate to the heart-rending emotional challenges families wrestle with during the organ transplant procedure. Comprehend the physical restrictions imposed on children by pulmonary hypertension and PVOD. Appreciate the critical role of sturdy support networks and trusty medical personnel in the face of daunting health dilemmas. Spark dialogue about the pressing imperatives of greater recognition and resources needed by families dealing with severe health situations. My special guest is Jan Stepps Life sometimes throws curveballs that test our strength and resilience. As a parent who has navigated the complex journey of her child's lung transplant, Jan Stepps is a beacon of hope and strength for all families facing similar situations. Armed with personal experience and the lessons learned from her daughter's PVOD diagnosis and subsequent transplant, Jan generously shares her insights on the emotional highs and lows of this life-changing journey. Once an accomplished train dispatcher, she adeptly uses her situational management skills, providing clarity amidst the chaos that such overwhelming situations create. The key moments in this episode are: 00:00:00 - Introduction, 00:04:33 - Initial Symptoms and Diagnosis, 00:07:40 - Pulmonary Hypertension and Transplant, 00:10:57 - Emotional Response and Coping, 00:13:55 - Supportive Network, 00:15:39 - Dealing with Difficult Conversations, 00:16:20 - Telling an Eleven-Year-Old, 00:18:40 - Understanding PVOD, 00:20:15 - Overwhelmed by Transplant Process, 00:26:30 - Finding Support in a Transplant Community, 00:32:28 - "The Importance of Keeping Promises", 00:33:45 - "The Transformation After the Lung Transplant", 00:35:09 - "Handling Follow-up Visits and Appointments", 00:36:24 - "Personal Growth and Perspective Shift", 00:38:47 - "Humor and Healing",   Connect with Jan   Instagram Facebook    Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here. Parents, download our free parent starter kit. When you download our starter kit, you'll learn how to: Give medicine to your child without it becoming a wrestling match Prepare your child (and yourself) for a shot so they can feel less anxious Create and use a coping plan for any medical appointment or procedure The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing. Child life specialists, get affordable PDUs on-demand here. Shop for your CLOC gear here.  

Today you'll learn about how doctors are successfully using double lung transplants for cancer patients, how blue whale behavior changes with environmental conditions, and how the history of the polygraph machine may have been based on a lie. Find episode transcripts here:  https://curiosity-daily-4e53644e.simplecast.com/episodes/double-lung-transplant-blue-whale-behavior-lie-detectorDouble Lung Transplant  “New double lung transplant technique is successful in two late-stage cancer patients.” by Kaitlin Sullivan and Kate Snow. 2023.https://www.nbcnews.com/health/cancer/new-double-lung-transplant-technique-successful-two-late-stage-cancer-rcna74886“250 days and counting: Waiting on new lungs after Covid.” by Erika Edwards. 2022.https://www.nbcnews.com/health/health-news/covid-lungs-patients-wait-new-lungs-covid-rcna22049“New guidelines would nearly double lung cancer screenings, benefit more women and Black people.” by Kelsie Sandoval. 2020.https://www.nbcnews.com/health/cancer/new-guidelines-would-nearly-double-lung-cancer-screenings-benefit-more-n1233069Cancer death rates are falling. Advances in lung cancer treatment are playing a major role.” by Erika Edwards. 2020.https://www.nbcnews.com/health/cancer/cancer-death-rates-are-falling-advances-lung-cancer-treatment-are-n1111706Blue Whale Behavior “Blue whale foraging and reproduction are related to environmental conditions, study shows” by OREGON STATE UNIVERSITYhttps://www.eurekalert.org/news-releases/981187“Environmental conditions and marine heatwaves influence blue whale foraging and reproductive effort” by Dawn R. Barlow et al.https://onlinelibrary.wiley.com/doi/10.1002/ece3.9770“Context-dependent variability in blue whale acoustic behaviour” by Leah A. Lewis et al.https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124089/“Blue Whale” by Discovery of Sound in the Sea and University of Rhode Islandhttps://dosits.org/galleries/audio-gallery/marine-mammals/baleen-whales/blue-whale/#:~:text=D%20calls%20are%20produced%20by,not%20have%20obvious%20geographic%20variation.“The IUCN Red List Categories and Criteria” by The IUCN Red Listhttps://www.iucnredlist.org/#:~:text=It%20divides%20species%20into%20nine,in%20the%20Wild%20and%20Extinct.Lie Detector“The Lie Detector Was Never Very Good at Telling the Truth” by Amit Katwalahttps://www.wired.com/story/lie-detector-never-very-good-at-telling-truth/“Lie Detectors Are Junk Science, but We Keep Using Them” by KATRINA GULLIVERhttps://reason.com/2023/03/07/lie-detectors-are-junk-science-but-we-keep-using-them/“What's the Deal with Lie Detectors?” by Michelle Kaminskyhttps://www.legalzoom.com/articles/whats-the-deal-with-lie-detectors#:~:text=Although%20the%20science%20is%20questionable,make%20people%20tell%20the%20truth.“The Effectiveness and Future of Polygraph Testing” by EBPSocietyhttps://www.ebpsociety.org/blog/education/444-the-effectiveness-and-future-of-polygraph-testingFollow Curiosity Daily on your favorite podcast app to get smarter with Calli and Nate — for free! Still curious? Get exclusive science shows, nature documentaries, and more real-life entertainment on discovery+! Go to https://discoveryplus.com/curiosity to start your 7-day free trial. discovery+ is currently only available for US subscribers.